Relevant bibliographies by topics / Resorcinaren

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Resorcinaren'

Author: Grafiati
Published: 4 June 2021
Last updated: 15 February 2022

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Journal articles on the topic "Resorcinaren"

1

Beyeh, Ngong K., Michael Kogej, Antti Åhman, Kari Rissanen, and Christoph A. Schalley. "Fliegende Kapseln: massenspektrometrische Detektion von Pyrogallaren- und Resorcinaren-Hexameren." Angewandte Chemie 118, no. 31 (2006): 5339–42. http://dx.doi.org/10.1002/ange.200600687.

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Ngurah, Budiana I. Gusti M., Jumina Jumina, Chairil Anwar, Mustofa Mustofa, and Sahadewa Sahadewa. "Synthesis of Benzoyl C-Phenylcalix[4]resorcinaryl Octaacetate and Cinnamoyl C-Phenylcalix[4]arene for UV Absorbers." Indonesian Journal of Chemistry 14, no. 2 (2014): 160–67. http://dx.doi.org/10.22146/ijc.21253.

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A new upper rim-functionalized benzoyl C-phenylcalix[4]resorcinaryl octaacetate and cinnamoyl C-phenylcalix[4]resorcinarene have been synthesized and evaluated as the absorbers for ultraviolet radiation. The benzoyl C-phenylcalix[4]resorcinaryl octaacetate was synthesized in 3 steps. They were synthesis of C-phenilcalix[4]resorcinarene via acid-catalyzed-condensation of resorcinol and benzaldehyde, followed by O-acetylation and Friedel-Craft benzoylation. The cinnamoyl C-phenylcalix[4]resorcinarene was synthesized in 4 steps. They were synthesis of C-phenilcalix[4]resorcinarene via acid-cataly
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Cortez-Maya, Sandra, Elena Klimova, R. I. Puente Lee, Andres Borja-Miranda, and Marcos Martinez-Garcia. "Synthesis and Characterization of Ferrocenyl Carboxilic Surface-Functionalized Resorcinaren-PAMAM Dendrimers." Current Organic Chemistry 19, no. 19 (2015): 1954–60. http://dx.doi.org/10.2174/1385272819666150604000213.

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Zhu, Sascha S, Holger Staats, Kai Brandhorst, et al. "Anionen bindende Resorcinaren-Cavitanden: die Bedeutung von CH⋅⋅⋅Anion-Wechselwirkungen." Angewandte Chemie 120, no. 4 (2008): 800–804. http://dx.doi.org/10.1002/ange.200703451.

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Velásquez-Silva, Betty Astrid, Alver Castillo-Aguirre, Zuly Jenny Rivera-Monroy, and Mauricio Maldonado. "Aminomethylated Calix[4]resorcinarenes as Modifying Agents for Glycidyl Methacrylate (GMA) Rigid Copolymers Surface." Polymers 11, no. 7 (2019): 1147. http://dx.doi.org/10.3390/polym11071147.

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Functionalization of tetrapropylcalix[4]resorcinarene, tetrapentylcalix[4]resorcinarene, tetranonylcalix[4]resorcinarene, and tetra-(4-hydroxyphenyl)calix[4]resorcinarene by means of aminomethylation reactions with the amino acids β-alanine and l-proline in the presence of aqueous formaldehyde was carried out. When β-alanine was used, the reaction products were tetrabenzoxazines. The reaction with tetra-(4-hydroxyphenyl)calix[4]resorcinarene did not proceed under the experimental conditions; therefore, l-proline was used, and the corresponding tetra-Mannich base was regio- and diasteroselectiv
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Dumoulin, Fabienne, Derya Topkaya, Songül Yaşar, Vefa Ahsen, and Ümit İşci. "Covalent or supramolecular combinations of resorcinarenes and porphyrinoids." Journal of Porphyrins and Phthalocyanines 20, no. 05 (2016): 571–81. http://dx.doi.org/10.1142/s108842461630010x.

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Cavitands and porphyrinoids are two major groups of molecules. If cyclodextrins are maybe the most famous type of cavitands, the properties of resorcinarenes are now well known and rise rapidly increasing attention. This mini-review aims at detailing all the combinations of resorcinarenes with porphyrinoids reported so far, evidencing the bright future of such combos. In addition, two newly synthesized porphyrins-resorcinarene hybrids are reported.
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Castillo-Aguirre and Maldonado. "Preparation of Methacrylate-based Polymers Modified with Chiral Resorcinarenes and Their Evaluation as Sorbents in Norepinephrine Microextraction." Polymers 11, no. 9 (2019): 1428. http://dx.doi.org/10.3390/polym11091428.

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Aminomethylation reactions between chiral amino compounds (S)-(-)-1-phenylethylamine and l-proline with tetranonylresorcinarene and tetra-(4-hydroxyphenyl)resorcinarene in presence of formaldehyde were studied. The reaction between l-proline and resorcinarenes generated regioselectively chiral tetra-Mannich bases, due to the molecular incorporation of the fragment of the chiral amino acid. On the other hand, tetranonylresorcinarene and (S)-(-)-1-phenylethylamine formed regio- and diasteroselectively chiral tetrabenzoxazines, both by chiral auxiliary functionalization and by the transformation
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Reynolds, Michael R., Fraser S. Pick, John J. Hayward, and John F. Trant. "A Concise Synthesis of a Methyl Ester 2-Resorcinarene: A Chair-Conformation Macrocycle." Symmetry 13, no. 4 (2021): 627. http://dx.doi.org/10.3390/sym13040627.

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Anions are important hydrogen bond acceptors in a range of biological, chemical, environmental and medical molecular recognition processes. These interactions have been exploited for the design and synthesis of ditopic resorcinarenes as the hydrogen bond strength can be tuned through the modification of the substituent at the 2-position. However, many potentially useful compounds, especially those incorporating electron-withdrawing functionalities, have not been prepared due to the challenge of their synthesis: their incorporation slows resorcinarene formation that is accessed by electrophilic
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Ngurah, Budiana I. Gusti M., Jumina Jumina, Chairil Anwar, Sunardi Sunardi, and Mustofa Mustofa. "Synthesis and In Vitro Evaluation of C-methylcalix[4]resorcinaryl octacinnamate and C-methylcalix[4]resorcinaryl octabenzoate as the Sunscreen." Indonesian Journal of Chemistry 17, no. 1 (2017): 63. http://dx.doi.org/10.22146/ijc.23575.

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The present study was aimed to synthesize and evaluate sunscreen activity of C-methylcalix[4]resorcinaryl octacinnamate and C-methylcalix[4]resorcinaryl octabenzoate. The target compounds were synthesized in 2 steps. They were a synthesis of C-methylcalix[4]-resorcinarene via acid catalyzed the condensation of resorcinol and acetaldehyde by using HCl catalyst, followed by esterification using cinnamoyl chloride and benzoyl chloride. The characterization of the target compounds was performed by IR, 1H-NMR, 13C-NMR, and LC-MS spectrometers. The sunscreen activity test was conducted by spectrosco
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Casas-Hinestroza, José Luis, Miguel Ángel Vela Suazo, and Mauricio Maldonado Villamil. "Experimental Comparative Study of Dynamic Behavior in Solution Phase of C-Tetra(phenyl)resorcin[4]arene and C-Tetra(phenyl)pyrogallol[4]arene." Molecules 25, no. 10 (2020): 2275. http://dx.doi.org/10.3390/molecules25102275.

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The synthesis of phenyl-resorcinarenes and pyrogallolarenes is known to produce a conformational mixture of cone and chair isomers. Depending on the synthesis conditions the composition of the conformational mixture is variable; however, the cone conformer is the greatest proportion of phenyl-resorcin[4]arenes and chair conformer of pyrogallol[4]arenes. The experimental evidence suggests that phenyl-substituted resorcinarene and pyrogallolarene exist as a dynamic boat in solution.
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Dissertations / Theses on the topic "Resorcinaren"

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Krause, Tilo. "Star Polymers and Dendrimers Based on Highly Functional Resorcin- and Pyrogallolarenes." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2007. http://nbn-resolving.de/urn:nbn:de:swb:14-1183015386384-28696.

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In the frame of this thesis different calix[4]resorcin- and calix[4]pyrogallolarene derivatives were used as platform for the synthesis of novel star polymers and dendritic structures. The objectives of this work can be portrayed under the following points: First: Synthesis and modification of calix[4]resorcin- and calix[4]pyrogallolarenes with a varying number and varying type of functional sites and their precise characterization by modern NMR techniques and single crystal X-ray diffraction. Second: Synthesis of well-defined star polymers and dendrimers with different number of arms and acco
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Krause, Tilo. "Star Polymers and Dendrimers Based on Highly Functional Resorcin- and Pyrogallolarenes." Doctoral thesis, Technische Universität Dresden, 2006. https://tud.qucosa.de/id/qucosa%3A24791.

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In the frame of this thesis different calix[4]resorcin- and calix[4]pyrogallolarene derivatives were used as platform for the synthesis of novel star polymers and dendritic structures. The objectives of this work can be portrayed under the following points: First: Synthesis and modification of calix[4]resorcin- and calix[4]pyrogallolarenes with a varying number and varying type of functional sites and their precise characterization by modern NMR techniques and single crystal X-ray diffraction. Second: Synthesis of well-defined star polymers and dendrimers with different number of arms and acco
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Vernetti, Samantha Sizemore. "Two New Resorcinarenes: A Pyridine & Acetic Acid Ligand for Metal Coordination and a Deep-Cavity Nitroquinoxaline Resorcinarene." Diss., CLICK HERE for online access, 2006. http://contentdm.lib.byu.edu/ETD/image/etd1279.pdf.

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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix(4)resorcinarene." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2001. http://nbn-resolving.de/urn:nbn:de:swb:14-994682363390-44859.

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In der vorliegenden Arbeit wird die Darstellung und Charakterisierung von aromatisch substituierten Calix(4)resorcinarenen behandelt. Im zweiten Kapitel werden die Grundlagen und Besonderheiten bei Calix(4)resorcinarenen angesprochen. Ein Überblick über die wichtigsten Verbindungen dieser Gruppe von Makrocyclen wird gegeben. Im Kapitel 3 werden wesentliche Methoden zur vollständigen O-Alkylierung bei Calix(4)resorcinaren genannt. Außerdem werden Methoden zur partiellen O-Alkylierung von C-Arylcalix(4)resorcinarenen vorgestellt. Das Kapitel 4 stellt die Methoden zur Strukturaufklärung mittels 2
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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix(4)resorcinarene." Doctoral thesis, Technische Universität Dresden, 2000. https://tud.qucosa.de/id/qucosa%3A24757.

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In der vorliegenden Arbeit wird die Darstellung und Charakterisierung von aromatisch substituierten Calix(4)resorcinarenen behandelt. Im zweiten Kapitel werden die Grundlagen und Besonderheiten bei Calix(4)resorcinarenen angesprochen. Ein Überblick über die wichtigsten Verbindungen dieser Gruppe von Makrocyclen wird gegeben. Im Kapitel 3 werden wesentliche Methoden zur vollständigen O-Alkylierung bei Calix(4)resorcinaren genannt. Außerdem werden Methoden zur partiellen O-Alkylierung von C-Arylcalix(4)resorcinarenen vorgestellt. Das Kapitel 4 stellt die Methoden zur Strukturaufklärung mittels 2
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Hong, Wei. "The chemistry of propargyl calix(4)resorcinarene." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ32484.pdf.

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Hünig, Hagen. "Darstellung und Charakterisierung neuartiger C-Arylcalix[4]resorcinarene." [S.l. : s.n.], 2001. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB9275691.

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Kleinhans, Dewald Johannes. "Studies in the selective synthesis of bidentate resorcinarene ligands." Thesis, Stellenbosch : University of Stellenbosch, 2010. http://hdl.handle.net/10019.1/4194.

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Thesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2010.<br>ENGLISH ABSTRACT: Resorcinarenes are macrocyclic products formed from the condensation of aldehydes (aliphatic or aromatic) and resorcinol and have been used in a wide range of applications since their first synthesis. Applications include: HPLC stationary phases for the separation of pyrimidine bases, racemic drugs and isomers, the selective extractions of lanthanides and actinides, as molecular receptors, catalysis, NMR chiral shift agents, GC separations and as starting materials for the synthesis of macr
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Boxhall, Jonathan Yates. "Synthetic routes towards chiral calix[4]resorcinarenes." Thesis, Loughborough University, 2003. https://dspace.lboro.ac.uk/2134/33906.

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This thesis is divided into three chapters. Chapter 1 contains a brief overview of the literature reports in the area of calix[4]resorcinarene chemistry. The many methods available for the preparation and use of these macrocycles, their functionalisation on both the upper and lower rims and the use of Mannich reaction protocols for the introduction of chirality into these symmetrical molecules are discussed. Chapter 2 describes new methodology for the formation of a range of chiral calix[4]resorcinarenes, most notably the formation of tetra alkyloxy calix[4]resorcinarenes as racemic mixtures,
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Chan, Yohan. "Some aspects of the chemistry of resorcinarenes." Thesis, Loughborough University, 2006. https://dspace.lboro.ac.uk/2134/34718.

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This thesis has been divided in three sections. The first chapter contains a review of resorcinarene chemistry. The second chapter contains the results and the discussion and the experimental details are provided in the third chapter. The first part of chapter two contains the results and discussion related to the synthesis of benzoxazines derived from resorcin[6]arene and resorcin[4]arene and the diastereoselectivity observed in the syntheses. The second part of chapter two describes the synthesis of inherently chiral resorcinarenes using non-chiral 3-alkyloxyphenols, the synthesis of benzoxa
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Book chapters on the topic "Resorcinaren"

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Wierzbicki, Michał, Hanna Jędrzejewska, and Agnieszka Szumna. "Chiral Calixarenes and Resorcinarenes." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_2.

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Tulli, Ludovico, and Patrick Shahgaldian. "Calixarenes and Resorcinarenes at Interfaces." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_37.

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Schneider, H. J., and U. Schneider. "The Host-Guest Chemistry of Resorcinarenes [1]." In Calixarenes 50th Anniversary: Commemorative Issue. Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0267-4_5.

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Botta, Maurizio, Maria Cristina De Rosa, Federico Corelli, Antonello Santini, and Andrea Tafi. "New C-Alkylcalix[4]Resorcinarenes: A Computational Study." In Fifth International Conference on the Spectroscopy of Biological Molecules. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1934-4_2.

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Arduini, A., A. Casnati, E. Dalcanale, A. Pochini, F. Ugozzoli, and R. Ungaro. "Calixarenes and Resorcinarenes in Molecular Recognition and Supramolecular Devices." In Supramolecular Science: Where It Is and Where It Is Going. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4554-1_5.

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Nicod, L., E. Gaubert, H. Barnier, and M. Lemaire. "Synthesis of Water Soluble Resorcinarenes Application in Nanofiltration-Complexation." In Molecular Recognition and Inclusion. Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-011-5288-4_76.

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Botta, M., M. Coppetti, P. Ricciardi, F. Corelli, and A. Tafi. "Artificial receptors: molecular modelling studies of calix[4]resorcinarene-capped porphyrins." In Spectroscopy of Biological Molecules: New Directions. Springer Netherlands, 1999. http://dx.doi.org/10.1007/978-94-011-4479-7_81.

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Tan, Daniel A., and Mauro Mocerino. "Calix[4]arenes and Resorcinarenes Bridged at the Wider Rim." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_10.

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Das, Sanjoy, and Malay K. Das. "Surface Modification of Resorcinarene-Based Self-Assembled Solid Lipid Nanoparticles for Drug Targeting." In Surface Modification of Nanoparticles for Targeted Drug Delivery. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-06115-9_16.

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Beyeh, Ngong Kodiah, and Kari Rissanen. "N-Alkyl Ammonium Resorcinarene Salts: A Versatile Family of Calixarene-Related Host Molecules." In Calixarenes and Beyond. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-31867-7_11.

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Conference papers on the topic "Resorcinaren"

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Kvasnica, Miroslav, and Byron W. Purse. "Synthesis of new resorcinarene-based molecular clips." In 15th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-15bmos-bmos2013_201391418945.

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Oh, Tae-Hwan, Ramakrishnan Ganesan, Je-Moon Yoon, and Jin-Baek Kim. "Negative nanomolecular resists based on Calix[4]resorcinarene." In SPIE 31st International Symposium on Advanced Lithography, edited by Qinghuang Lin. SPIE, 2006. http://dx.doi.org/10.1117/12.660111.

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Okuyama, Kenichi. "Molecular resists based on calix[4]resorcinarene derivatives for EB lithography." In SPIE Advanced Lithography, edited by Clifford L. Henderson. SPIE, 2009. http://dx.doi.org/10.1117/12.813632.

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Ariyanti, Dita, Jumina, Dyah Iswantini, Purwantiningsih, Novik Nurhidayat, and Hefni Effendi. "The synthesized sunscreen compounds: C-heptylcalix[4]resorcinarene octabenzoate and octasinnamate." In 3RD INTERNATIONAL CONFERENCE ON CHEMISTRY, CHEMICAL PROCESS AND ENGINEERING (IC3PE). AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0062413.

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Handayani, Santi Nur, Heny Ekowati, Irmanto, Della Nadya Ayu Aprilia, and Silva Utami. "Synthesis of phenylcalix[4]resorcinarena sulfonate and it’s aplication as an antioxidant." In THE 14TH JOINT CONFERENCE ON CHEMISTRY 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0006139.

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Şen, Sibel, Rifat Çapan, and Gülen Türker. "Thin film properties and the detection volatile organic compounds of C-methylcalix(4)resorcinarene." In SolarPACES 2017: International Conference on Concentrating Solar Power and Chemical Energy Systems. Author(s), 2018. http://dx.doi.org/10.1063/1.5078881.

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Etika, Sri Benti, Edi Nasra, Abdul Hafids, and T. K. Sari. "Utilization of C-Cinnamal Calix[4] Resorcinarene as Adsorbent for Rhodamin B and Methanil Yellow." In International Conference on Biology, Sciences and Education (ICoBioSE 2019). Atlantis Press, 2020. http://dx.doi.org/10.2991/absr.k.200807.047.

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Paviet-Hartmann, Patricia, Jared Horkley, Joshua Pak, Eric Brown, and Terry Todd. "Resorcinarenes and Aza-crowns as New Extractants for the Separation of Technetium-99." In 2008 MRS Fall Meetin. Materials Research Society, 2008. http://dx.doi.org/10.1557/proc-1124-q10-04.

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Wallace, W. E., K. M. Flynn, C. M. Guttman, et al. "Quantitative measurement of the molecular-mass distribution in calix[4]resorcinarene molecular glass resists by mass spectrometry." In SPIE Advanced Lithography, edited by Clifford L. Henderson. SPIE, 2009. http://dx.doi.org/10.1117/12.813680.

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Echigo, Masatoshi, and Dai Oguro. "Development of new phenylcalix[4]resorcinarene: its application to positive-tone molecular resist for EB and EUV lithography." In SPIE Advanced Lithography, edited by Clifford L. Henderson. SPIE, 2009. http://dx.doi.org/10.1117/12.813487.

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